ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test
Introduction to the ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test
The ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with glycosylation disorders. These disorders can lead to severe metabolic issues, and early detection is vital for effective management and treatment. This test employs Next-Generation Sequencing (NGS) technology, which allows for a comprehensive analysis of the ALG8 gene, crucial for proper glycosylation processes in the body.
What the Test Measures
This genetic test specifically detects mutations in the ALG8 gene, which plays a critical role in the glycosylation pathway. By analyzing the DNA, the test can identify any alterations that may lead to metabolic disorders, providing essential insights into a patient’s health.
Who Should Consider This Test?
Individuals who should consider the ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test include:
- Those with a family history of glycosylation disorders.
- Patients showing symptoms of metabolic disorders, such as developmental delays, neurological issues, or unexplained health conditions.
- Individuals seeking genetic counseling for family planning or to understand their risks.
Benefits of Taking the Test
Taking the ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test offers numerous benefits:
- Early diagnosis of potential metabolic disorders.
- Informed decision-making regarding treatment options.
- Guidance for family planning and understanding hereditary risks.
- Access to specialized care and support from healthcare professionals.
Understanding Your Results
After the test is conducted, results are typically available within 3 to 4 weeks. A healthcare provider will assist in interpreting the results, explaining the implications of any detected mutations, and discussing potential next steps for management or treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Pre-Test Instructions
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card.
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by Glycosylation Disorder Type 1H.
Book Your Test Today!
At DNA Labs Kenya, we have branches across all major cities, including Nairobi, Mombasa, and Kisumu, ensuring easy access to our services. For your convenience, we also offer home sample collection services. Don’t wait any longer; book your ALG8 Gene Glycosylation Disorder Type 1H NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.
